OXOS MC2 Portable X-Ray System Recall
Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product Descr
Updated June 11, 2026
The OXOS Medical MC2 Portable X-Ray System is being recalled due to a defective circuit board that can overheat. The device may pose a fire or burn risk to clinicians and patients during use.
Is the Oxos Medical Inc recalled? Yes. This product was recalled by FDA on June 11, 2026. Details below.
What is recalled
OXOS Medical MC2 Portable X-Ray System, Model MC2 and MC2.1, Software Version 5.7.0. This is a portable, handheld x-ray system used for diagnostic imaging of extremities and shoulders.
Am I affected
You're affected if you own or operate an OXOS Medical MC2 Portable X-Ray System with Model MC2 or MC2.1 and Software Version 5.7.0. Check your device label for the model and software version.
What to do right now
Stop using the MC2 Portable X-Ray System immediately. Contact OXOS Medical, Inc directly for repair or replacement instructions. Do not attempt to operate the device until you have received guidance from the manufacturer.
The hazard
Due to a defective circuit board that overheats
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-2857-2026
- Classification
- Class II
- Recalled
- June 11, 2026
Get free recall alerts
New Medical Devices recalls, the moment they post.
Free forever. Unsubscribe anytime. We never sell your data.
More Medical Devices recalls
Siemens Atellica CH Urine Albumin Recall
Siemens Atellica CH Urine Albumin test kits may produce falsely low results for urea nitrogen and hemoglobin A1c levels, or experience delayed results due to …
Siemens Healthcare Diagnostics, Inc.
Boston Scientific Rapid Refill Injection System Recall
Boston Scientific's Rapid Refill Continuous Injection System contains a recalled syringe component that may loosen or disconnect from the manifold. This can …
Boston Scientific Corporation
Syva Emit Tox Serum Tricyclic Recall
Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2 contains an out-of-specification concentration of sodium azide. Lab technicians may …
Siemens Healthcare Diagnostics, Inc.